Genes, Chromosomes and Cancer, 1045-2257

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  1. 2021
  2. Genomic and transcriptomic characterization of desmoplastic small round cell tumors

    Saskia Sydow, Yvonne M.H. Versleijen-Jonkers, Magnus Hansson, Anke E.M. van Erp, Melissa H.S. Hillebrandt-Roeffen, Winette T.A. van der Graaf, Paul Piccinelli, Pehr Rissler, Uta E. Flucke & Fredrik Mertens, 2021 Apr 30, In: Genes Chromosomes and Cancer.

    Research output: Contribution to journalArticle

  3. Single-cell sequencing in translational cancer research and challenges to meet clinical diagnostic needs

    Ulrich Pfisterer, Julia Bräunig, Per Brattås, Markus Heidenblad, Göran Karlsson & Thoas Fioretos, 2021 Feb 21, In: Genes, Chromosomes and Cancer.

    Research output: Contribution to journalReview article

  4. Clinical and genomic characterization of patients diagnosed with the provisional entity Acute myeloid leukemia with BCR-ABL1, a Swedish population-based study

    Christina Orsmark-Pietras, Niklas Landberg, Fryderyk Lorenz, Bertil Uggla, Martin Höglund, Sören Lehmann, Åsa Derolf, Stefan Deneberg, Petar Antunovic, Jörg Cammenga, Lars Möllgård, Lovisa Wennström, Henrik Lilljebjörn, Marianne Rissler, Thoas Fioretos & Vladimir Lj Lazarevic, 2021 Jan 12, In: Genes, Chromosomes and Cancer.

    Research output: Contribution to journalArticle

  5. 2020
  6. Deep sequencing of myxoinflammatory fibroblastic sarcoma

    Elsa Arbajian, Jakob Hofvander, Linda Magnusson & Fredrik Mertens, 2020 May, In: Genes, Chromosomes and Cancer. 59, 5, p. 309-317 9 p.

    Research output: Contribution to journalArticle

  7. SFPQ-ABL1-positive B-cell precursor acute lymphoblastic leukemias

    Andrea Biloglav, LINDA OLSSON, Johan Theander, Mikael Behrendtz, Anders Castor & Bertil Johansson, 2020 Apr 19, In: Genes, Chromosomes and Cancer.

    Research output: Contribution to journalLetter

  8. Farewell message from the Editor-in-Chief of Genes, Chromosomes & Cancer

    Felix Mitelman, 2020, In: Genes Chromosomes and Cancer. 59, 1, p. 3-4 2 p.

    Research output: Contribution to journalDebate/Note/Editorial

  9. 2019
  10. Most gene fusions in cancer are stochastic events

    Bertil Johansson, Fredrik Mertens, Tommy Schyman, Jonas Björk, Nils Mandahl & Felix Mitelman, 2019 Sep, In: Genes Chromosomes and Cancer. 58, 9, p. 607-611 5 p.

    Research output: Contribution to journalArticle

  11. Cancer chromosome breakpoints cluster in gene-rich genomic regions

    Felix Mitelman, Bertil Johansson, Fredrik Mertens, Tommy Schyman & Nils Mandahl, 2019, In: Genes Chromosomes and Cancer. 58, 3, p. 149-154

    Research output: Contribution to journalArticle

  12. Clonal evolution through genetic bottlenecks and telomere attrition: Potential threats to in vitro data reproducibility

    David Gisselsson, Daniel Lichtenzstejn, Polina Kachko, Jenny Karlsson, Esther Manor & Sabine Mai, 2019, In: Genes Chromosomes and Cancer. 58, 7, p. 452-461

    Research output: Contribution to journalReview article

  13. Genetic profiling of a chondroblastoma-like osteosarcoma/malignant phosphaturic mesenchymal tumor of bone reveals a homozygous deletion of CDKN2A, intragenic deletion of DMD, and a targetable FN1-FGFR1 gene fusion

    Karim H Saba, Louise Cornmark, Marianne Rissler, Thoas Fioretos, Kristina Åström, Felix Haglund, Andrew E Rosenberg, Otte Brosjö & Karolin H Nord, 2019, In: Genes, Chromosomes and Cancer. 58, 10, p. 731-736

    Research output: Contribution to journalArticle

  14. 2018
  15. Telomere length, telomerase reverse transcriptase promoter mutations, and melanoma risk

    Sivaramakrishna Rachakonda, Haiying Kong, Nalini Srinivas, Zaida Garcia-Casado, Celia Requena, Mahdi Fallah, Barbara Heidenreich, Dolores Planelles, Victor Traves, Dirk Schadendorf, Eduardo Nagore & Rajiv Kumar, 2018 Nov, In: Genes, Chromosomes and Cancer. 57, 11, p. 564-572 9 p.

    Research output: Contribution to journalArticle

  16. A field guide for cancer diagnostics using cell-free DNA: From principles to practice and clinical applications

    Anna Lena Volckmar, Holger Sültmann, Anja Riediger, Thoas Fioretos, Peter Schirmacher, Volker Endris, Albrecht Stenzinger & Steffen Dietz, 2018 Mar 1, In: Genes Chromosomes and Cancer. 57, 3, p. 123-139 17 p.

    Research output: Contribution to journalReview article

  17. 2017
  18. Soft tissue angiofibroma: Clinicopathologic, immunohistochemical and molecular analysis of 14 cases

    Elise M. Bekers, Patricia J.T.A. Groenen, Marian A.J. Verdijk, Winny L. Raaijmakers-van Geloof, Paul Roepman, Robert Vink, Nathalie D.B. Gilhuijs, Joost M. van Gorp, Judith V M G Bovée, David H. Creytens, Adrienne M. Flanagan, Albert J. H. Suurmeijer, Thomas Mentzel, Elsa Arbajian & Uta Flucke, 2017 Oct 1, In: Genes Chromosomes and Cancer. 56, 10, p. 750-757 8 p.

    Research output: Contribution to journalArticle

  19. Pediatric T-cell acute lymphoblastic leukemia

    Kristina Karrman & Bertil Johansson, 2017 Feb 1, In: Genes Chromosomes and Cancer. 56, 2, p. 89-116 28 p.

    Research output: Contribution to journalReview article

  20. 2016
  21. Trisomy 8 in pediatric acute myeloid leukemia: A NOPHO-AML study

    Anne Cathrine Lund Laursen, Julie Damgaard Sandahl, Eigil Kjeldsen, Jonas Abrahamsson, Peter Asdahl, Shau Yin Ha, Jesper Heldrup, Kirsi Jahnukainen, Ólafur G. Jónsson, Birgitte Lausen, Josefine Palle, Bernward Zeller, Erik Forestier & Henrik Hasle, 2016 Sep 1, In: Genes Chromosomes and Cancer. 55, 9, p. 719-726 8 p.

    Research output: Contribution to journalArticle

  22. Gene fusions in soft tissue tumors: Recurrent and overlapping pathogenetic themes.

    Fredrik Mertens, Cristina R Antonescu & Felix Mitelman, 2016, In: Genes, Chromosomes and Cancer. 55, 4, p. 291-310

    Research output: Contribution to journalReview article

  23. 2015
  24. A Population-Based Single Nucleotide Polymorphism Array Analysis of Genomic Aberrations in Younger Adult Acute Lymphoblastic Leukemia Patients

    Vaidas Dirse, Agne Bertasiute, Egle Gineikiene, Tadas Zvirblis, Ruta Dambrauskiene, Rolandas Gerbutavicius, Elona Juozaityte, Ligita Malciute, Kajsa Paulsson & Laimonas Griskevicius, 2015, In: Genes, Chromosomes and Cancer. 54, 5, p. 326-333

    Research output: Contribution to journalArticle

  25. Cooperative genetic changes in pediatric B-cell precursor acute lymphoblastic leukemia with deletions or mutations of IKZF1.

    Linda Olsson, Ferras Albitar, Anders Castor, Mikael Behrendtz, Andrea Biloglav, Kajsa Paulsson & Bertil Johansson, 2015, In: Genes, Chromosomes and Cancer. 54, 5, p. 315-325

    Research output: Contribution to journalArticle

  26. Impact of a paternal origin of germline BRCA1/2 mutations on the age at breast and ovarian cancer diagnosis in a Southern Swedish cohort.

    Carolina Ellberg, Helena Jernström, Per Broberg, Åke Borg & Håkan Olsson, 2015, In: Genes, Chromosomes and Cancer. 54, 1, p. 39-50

    Research output: Contribution to journalArticle

  27. Metabolic gene variants associated with chromosomal aberrations in healthy humans.

    Kari Hemminki, Christoph Frank, Asta Försti, Ludovit Musak, Alena Kazimirova, Magdalena Barancokova, Alexandra Horska, Veronika Vymetalkova, Zdenek Smerhovsky, Alessio Naccarati, Pavel Soucek, Ludmila Vodickova, Janka Buchancova, Bozena Smolkova, Maria Dusinska & Pavel Vodicka, 2015, In: Genes, Chromosomes and Cancer. 54, 4, p. 260-266

    Research output: Contribution to journalArticle

  28. Ring chromosomes, breakpoint clusters, and neocentromeres in sarcomas.

    Gemma Macchia, Karolin Hansén Nord, Monica Zoli, Stefania Purgato, Pietro D'Addabbo, Christopher W Whelan, Lucia Carbone, Giovanni Perini, Fredrik Mertens, Mariano Rocchi & Clelia Tiziana Storlazzi, 2015, In: Genes, Chromosomes and Cancer. 54, 3, p. 156-167

    Research output: Contribution to journalArticle

  29. 2014
  30. Amplification of 2p as a genomic marker for transformation in lymphoma

    Anna Kwiecinska, Koichi Ichimura, Mattias Berglund, Andrii Dinets, Luqman Sulaiman, V. Peter Collins, Catharina Larsson, Anna Porwit & Svetlana Bajalica Lagercrantz, 2014, In: Genes Chromosomes and Cancer. 53, 9, p. 750-768 19 p.

    Research output: Contribution to journalArticle

  31. Clear cell sarcoma of the kidney demonstrates an embryonic signature indicative of a primitive nephrogenic origin.

    Jenny Karlsson, Linda Holmquist Mengelbier, Cristina Ciornei, Arlene Naranjo, Maureen J O'Sullivan & David Gisselsson Nord, 2014, In: Genes, Chromosomes and Cancer. 53, 5, p. 381-391

    Research output: Contribution to journalArticle

  32. Exomic analysis of myxoid liposarcomas, synovial sarcomas, and osteosarcomas

    Christine G. Joseph, Heejung Hwang, Yuchen Jiao, Laura D. Wood, Isaac Kinde, Jian Wu, Nils Mandahl, Jinyong Luo, Ralph H. Hruban, Luis A. Diaz Jr, Tong-Chuan He, Bert Vogelstein, Kenneth W. Kinzler, Fredrik Mertens & Nickolas Papadopoulos, 2014, In: Genes, Chromosomes and Cancer. 53, 1, p. 15-24

    Research output: Contribution to journalArticle

  33. Ploidy and clinical characteristics of childhood acute myeloid leukemia: A NOPHO-AML study

    Julie Damgaard Sandahl, Eigil Kjeldsen, Jonas Abrahamsson, Shau-Yin Ha, Jesper Heldrup, Kirsi Jahnukainen, Olafur G. Jonsson, Birgitte Lausen, Josefine Palle, Bernward Zeller, Erik Forestier & Henrik Hasle, 2014, In: Genes, Chromosomes and Cancer. 53, 8, p. 667-675

    Research output: Contribution to journalArticle

  34. 2013
  35. Comprehensive genetic analysis identifies a pathognomonic NAB2/STAT6 fusion gene, nonrandom secondary genomic imbalances, and a characteristic gene expression profile in solitary fibrous tumor.

    Arezoo Mohajeri, Johnbosco Tayebwa, Anna Collin, Jenny Nilsson, Linda Magnusson, Fredrik Vult von Steyern, Otte Brosjö, Henryk Domanski, Olle Larsson, Raf Sciot, Maria Debiec-Rychter, Jason L Hornick, Nils Mandahl, Karolin Hansén Nord & Fredrik Mertens GCC Klinisk genetik, 2013, In: Genes, Chromosomes and Cancer. 52, 10, p. 873-886

    Research output: Contribution to journalArticle

  36. 2012
  37. Amplification and overexpression of the ABCC3 (MRP3) gene in primary breast cancer

    Laura Partanen, Johan Staaf, Minna Tanner, Vilppu J. Tuominen, Åke Borg & Jorma Isola, 2012, In: Genes, Chromosomes and Cancer. 51, 9, p. 832-840

    Research output: Contribution to journalArticle

  38. Copy Number Defects of G1-Cell Cycle Genes in Neuroblastoma are Frequent and Correlate with High Expression of E2F Target Genes and a Poor Prognosis

    Jan J. Molenaar, Jan Koster, Marli E. Ebus, Peter van Sluis, Ellen M. Westerhout, Katleen de Preter, David Gisselsson Nord, Ingrid Øra, Frank Speleman, Huib N. Caron & Rogier Versteeg, 2012, In: Genes, Chromosomes and Cancer. 51, 1, p. 10-19

    Research output: Contribution to journalArticle

  39. Fusion of the AHRR and NCOA2 genes through a recurrent translocation t(5;8)(p15;q13) in soft tissue angiofibroma results in upregulation of aryl hydrocarbon receptor target genes.

    Yuesheng Jin, Emely Möller, Karolin Hansén Nord, Nils Mandahl, Fredrik Vult von Steyern, Henryk Domanski, Adrian Mariño-Enríquez, Linda Magnusson, Jenny Nilsson, Raf Sciot, Christopher D M Fletcher, Maria Debiec-Rychter & Fredrik Mertens, 2012, In: Genes, Chromosomes and Cancer. 51, 5, p. 510-520

    Research output: Contribution to journalArticle

  40. High frequency of BTG1 deletions in acute lymphoblastic leukemia in children with down syndrome.

    Catarina Lundin, Lars Hjorth, Mikael Behrendtz, Ann Nordgren, Lars Palmqvist, Mette Klarskov Andersen, Andrea Biloglav, Erik Forestier, Kajsa Paulsson & Bertil Johansson, 2012, In: Genes, Chromosomes and Cancer. 51, p. 196-206

    Research output: Contribution to journalArticle

  41. Identification of a novel, recurrent HEY1-NCOA2 fusion in mesenchymal chondrosarcoma based on a genome-wide screen of exon-level expression data

    Lu Wang, Toru Motoi, Raya Khanin, Adam Olshen, Fredrik Mertens, Julia Bridge, Paola Dal Cin, Cristina R. Antonescu, Samuel Singer, Meera Hameed, Judith V. M. G. Bovee, Pancras C. W. Hogendoorn, Nicholas Socci & Marc Ladanyi, 2012, In: Genes, Chromosomes and Cancer. 51, 2, p. 127-139

    Research output: Contribution to journalArticle

  42. Telomere length and LINE1 methylation is associated with chromosomal aberrations in peripheral blood.

    Huiqi Li, Hilde Tveitan Hilmarsen, Mohammad Bakhtiar Hossain, Jonas Björk, Inger-Lise Hansteen, Maria Albin, Camilla Furu Skjelbred & Karin Broberg Palmgren, 2012, In: Genes, Chromosomes and Cancer.

    Research output: Contribution to journalArticle

  43. 2011
  44. Alternative lengthening of telomeres-An enhanced chromosomal instability in aggressive non-MYCN amplified and telomere elongated neuroblastomas.

    Gisela Lundberg, Daniel Sehic, John-Kalle Länsberg, Ingrid Øra, Attila Frigyesi, Victoria Castel, Samuel Navarro, Marta Piqueras, Tommy Martinsson, Rosa Noguera & David Gisselsson Nord, 2011, In: Genes, Chromosomes and Cancer. 50, 4, p. 250-262

    Research output: Contribution to journalArticle

  45. Fusion Gene Microarray Reveals Cancer Type-Specificity Among Fusion Genes

    Marthe Lovf, Gard O. S. Thomassen, Anne Cathrine Bakken, Ricardo Celestino, Thoas Fioretos, Guro E. Lind, Ragnhild A. Lothe & Rolf I. Skotheim, 2011, In: Genes, Chromosomes and Cancer. 50, 5, p. 348-357

    Research output: Contribution to journalArticle

  46. Gene expression and single nucleotide polymorphism array analyses of spindle cell lipomas and conventional lipomas with 13q14 deletion.

    Hammurabi Bartuma, Karolin Hansén Nord, Gemma Macchia, Margareth Isaksson, Jenny Nilsson, Henryk Domanski, Nils Mandahl & Fredrik Mertens, 2011, In: Genes, Chromosomes and Cancer. 50, p. 619-632

    Research output: Contribution to journalArticle

  47. High-resolution genomic screening in mantle cell lymphoma--specific changes correlate with genomic complexity, the proliferation signature and survival.

    Anna M. Halldórsdóttir, Birgitta Sander, Hanna Göransson, Anders Isaksson, Eva Kimby, Mahmoud Mansouri, Richard Rosenquist & Hans Ehrencrona, 2011, In: Genes, Chromosomes and Cancer. 50, 2, p. 113-121

    Research output: Contribution to journalArticle

  48. Prognostic Value of SOX2 Expression in Neuroblastoma

    Maria del Carmen Gomez-Mateo, Marta Piqueras, Victoria Castel, Sven Påhlman, Rosa Noguera & Samuel Navarro, 2011, In: Genes, Chromosomes and Cancer. 50, 5, p. 374-377

    Research output: Contribution to journalLetter

  49. 2010
  50. Genomic alterations in histopathologically normal breast tissue from BRCA1 mutation carriers may be caused by BRCA1 haploinsufficiency.

    Karin Rennstam, Anita Ringberg, Heather E Cunliffe, Håkan Olsson, Göran Landberg & Ingrid Hedenfalk, 2010, In: Genes, Chromosomes and Cancer. 49, p. 78-90

    Research output: Contribution to journalArticle

  51. Polymorphisms in the Transforming Growth Factor Beta 1 Pathway in Relation to Colorectal Cancer Progression

    Asta Foersti, Xuchen Li, Kerstin Wagner, Bjorn Tavelin, Kerstin Enquist, Richard Palmqvist, Andrea Altieri, Goran Hallmans, Kari Hemminki & Per Lenner, 2010, In: Genes, Chromosomes and Cancer. 49, 3, p. 270-281

    Research output: Contribution to journalArticle

  52. 2009
  53. Characterization of a Hotspot Region on Chromosome 12 for Amplification in Ring Chromosomes in Atypical Lipomatous Tumors

    Domenico Trombetta, Fredrik Mertens, Angelo Lonoce, Pietro D'Addabbo, Karin Rennstam, Nils Mandahl & Clelia Tiziana Storlazzi, 2009, In: Genes, Chromosomes and Cancer. 48, 11, p. 993-1001

    Research output: Contribution to journalArticle

  54. Clinical and cytogenetic features of a population-based consecutive series of 285 pediatric T-cell acute lymphoblastic leukemias: Rare T-cell receptor gene rearrangements are associated with poor outcome.

    Kristina Karrman, Erik Forestier, Mats Heyman, Mette K Andersen, Kirsi Autio, Elisabeth Blennow, Georg Borgström, Hans Ehrencrona, Irina Golovleva, Sverre Heim, Kristiina Heinonen, Randi Hovland, Johann H Johannsson, Gitte Kerndrup, Ann Nordgren, Lars Palmqvist & Bertil Johansson, 2009, In: Genes, Chromosomes and Cancer. 48, 9, p. 795-805

    Research output: Contribution to journalArticle

  55. Cytogenetic Analysis of 101 Giant Cell Tumors of Bone: Nonrandom Patterns of Telomeric Associations and Other Structural Aberrations

    Ludmila Gorunova, Fredrik Vult von Steyern, Tiziana Storlazzi, Bodil Bjerkehagen, Gunnar Folleras, Sverre Heim, Nils Mandahl & Fredrik Mertens, 2009, In: Genes, Chromosomes and Cancer. 48, 7, p. 583-602

    Research output: Contribution to journalArticle

  56. High hyperdiploid childhood acute lymphoblastic leukemia.

    Kajsa Paulsson & Bertil Johansson, 2009, In: Genes, Chromosomes and Cancer. 48, p. 637-660

    Research output: Contribution to journalArticle

  57. No Genomic Aberrations in Langerhans Cell Histiocytosis as Assessed by Diverse Molecular Technologies

    Cristiana E. T. da Costa, Karoly Szuhai, Ronald van Eijk, Manja Hoogeboom, Raphael Sciot, Fredrik Mertens, Helga Bjorgvinsdottir, Maria Debiec-Rychter, Ronald R. de Krijger, Pancras C. W. Hogendoorn, R. Maarten Egeler & Nicola E. Annels, 2009, In: Genes, Chromosomes and Cancer. 48, 3, p. 239-249

    Research output: Contribution to journalArticle

  58. t(19;22)(q13;q12) Translocation Leading to the Novel Fusion Gene EWSRI-ZNF444 in Soft Tissue Myoepithelial Carcinoma

    Petter Brandal, Ioannis Panagopoulos, Bodil Bjerkehagen & Sverre Heim, 2009, In: Genes, Chromosomes and Cancer. 48, 12, p. 1051-1056

    Research output: Contribution to journalArticle

  59. 2008
  60. A PCR/restriction digestion assay for the detection of the transcript variants 1 and 2 of POU5F1.

    Ioannis Panagopoulos, Emely Möller, Margareth Isaksson & Fredrik Mertens, 2008, In: Genes, Chromosomes and Cancer. 47, p. 521-529

    Research output: Contribution to journalArticle

  61. Clinical and cytogenetic features of pediatric dic(9;20)(p13.2;q11.2)-positive B-Cell precursor acute lymphoblastic leukemias: A nordic series of 24 cases and review of the literature

    Erik Forestier, Fredrika Gauffin, Mette K. Andersen, Kirsi Autio, Georg Borgstrom, Irina Golovleva, Britt Gustafsson, Sverre Heim, Kristina Heinonen, Mats Heyman, Randi Hovland, Johann H. Johannsson, Gitte Kerndrup, Richard Rosenquist, Jacqueline Schoumans, Birgitta Swolin, Bertil Johansson & Ann Nordgren, 2008, In: Genes, Chromosomes and Cancer. 47, 2, p. 149-158

    Research output: Contribution to journalReview article

  62. Detection of a t(1;22)(q23;q 12) translocation leading to an EWSR1-PBX1 fusion gene in a myoepithelioma

    Petter Brandal, Ioannis Panagopoulos, Bodil Bjerkehagen, Ludmilla Gorunova, Sigmund Skjeldal, Francesca Micci & Sverre Heim, 2008, In: Genes, Chromosomes and Cancer. 47, 7, p. 558-564

    Research output: Contribution to journalArticle

  63. High-resolution molecular cytogenetic analysis of Wilms tumors highlights diagnostic difficulties among small round cell kidney tumors.

    Ylva Stewénius, Yuesheng Jin, Ingrid Øra, Ioannis Panagopoulos, Emely Möller, Fredrik Mertens, Bengt Sandstedt, Jan Alumets, Måns Åkerman, Johannes Hm Merks, Jan de Kraker & David Gisselsson Nord, 2008, In: Genes, Chromosomes and Cancer. 47, 10, p. 845-852

    Research output: Contribution to journalArticle

  64. Molecular identification of COL6A3-CSF1 fusion transcripts in tenosynovial giant cell tumors

    Emely Möller, Nils Mandahl, Fredrik Mertens & Ioannis Panagopoulos, 2008, In: Genes, Chromosomes and Cancer. 47, 1, p. 21-25

    Research output: Contribution to journalArticle

  65. Mutations of FLT3, NRAS, KRAS, and PTPN11 are frequent and possibly mutually exclusive in high hyperdiploid childhood acute lymphoblastic leukemia

    Kajsa Paulsson, Andrea Biloglav, Bodil Strömbeck, Fredrik Nilsson, Jesper Heldrup, Mikael Behrendtz, Erik Forestier, Anna Andersson, Thoas Fioretos & Bertil Johansson, 2008, In: Genes, Chromosomes and Cancer. 47, 1, p. 26-33

    Research output: Contribution to journalArticle

  66. Promoter analysis of epigenetically controlled genes in bladder cancer.

    Srinivas Veerla, Ioannis Panagopoulos, Yuesheng Jin, David Lindgren & Mattias Höglund, 2008, In: Genes, Chromosomes and Cancer. 47, p. 368-378

    Research output: Contribution to journalArticle

  67. Screening for copy-number alterations and loss of heterozygosity in chronic lymphocytic leukemia-A comparative study of four differently designed, high resolution microarray platforms.

    Rebeqa Gunnarsson, Johan Staaf, Mattias Jansson, Anne Marie Ottesen, Hanna Göransson, Ulrika Liljedahl, Ulrik Ralfkiær, Mahmoud Mansouri, Anne Mette Buhl, Karin Ekström Smedby, Henrik Hjalgrim, Ann-Christine Syvänen, Åke Borg, Anders Isaksson, Jesper Jurlander, Gunnar Juliusson & Richard Rosenquist, 2008, In: Genes, Chromosomes and Cancer. 47, 8, p. 697-711

    Research output: Contribution to journalArticle

  68. 2007
  69. Assessment of the clinical and molecular impact of different cytogenetic subgroups in a series of 272 lipomas with abnormal karyotype

    Hammurabi Bartuma, Karolin Hansén Nord, Ioannis Panagopoulos, Anna Collin, Anders Rydholm, Pelle Gustafson, Henrik C F Bauer, Otte Brosjö, Henryk A Domanski, Nils Mandahl & Fredrik Mertens, 2007 Jun, In: Genes, Chromosomes and Cancer. 46, 6, p. 594-606 13 p.

    Research output: Contribution to journalArticle

  70. Characterization of the native CREB3L2 transcription factor and the FUS/CREB3L2 chimera

    Ioannis Panagopoulos, Emely Möller, Anna Dahlén, Margareth Isaksson, Nils Mandahl, Alexios Vlamis-Gardikas & Fredrik Mertens, 2007 Feb, In: Genes, Chromosomes and Cancer. 46, 2, p. 181-191 11 p.

    Research output: Contribution to journalArticle

  71. Cytogenetic patterns in ETV6/RUNX1-positive pediatric B-cell precursor acute lymphoblastic leukemia: A Nordic series of 245 cases and review of the literature

    Erik Forestier, Mette K. Andersen, Kirsi Autio, Elisabeth Blennow, Georg Borgstrom, Irina Golovleva, Sverre Heim, Kristina Heinonen, Randi Hovland, Johann H. Johannsson, Gitte Kerndrup, Ann Nordgren, Richard Rosenquist, Birgitta Swolin & Bertil Johansson, 2007, In: Genes, Chromosomes and Cancer. 46, 5, p. 440-450

    Research output: Contribution to journalReview article

  72. Proposals for standardized Protocols for cytogenetic analyses of acute leukemias, chronic lymphocytic leukemia, chronic myeloid leukemia, chronic myeloproliferative disorders, and myelodysplastic syndromes

    Claudia Haferlach, Harald Rieder, Debra M. Lillington, Nicole Dastugue, Anne Hagemeijer, Jochen Harbott, Stephan Stilgenbauer, Sakari Knuutila, Bertil Johansson & Christa Fonatsch, 2007, In: Genes, Chromosomes and Cancer. 46, 5, p. 494-499

    Research output: Contribution to journalArticle

  73. Response to letter by the ISCN standing committee

    Felix Mitelman & Janet D. Rowley, 2007, In: Genes, Chromosomes and Cancer. 46, 5, p. 516-516

    Research output: Contribution to journalLetter

  74. 2006
  75. Confirmation of the high frequency of the TMPRSS2/ERG fusion gene in prostate cancer.

    Maria Soller, Margareth Isaksson, Peter Elfving, Wolfgang Soller, Rolf Lundgren & Ioannis Panagopoulos, 2006, In: Genes, Chromosomes and Cancer. 45, 7, p. 717-719

    Research output: Contribution to journalLetter

  76. Translocation-excision-deletion-amplification mechanism leading to nonsyntenic coamplification of MYC and ATBF1

    N Van Roy, J Vandesompele, B Menten, Helén Nilsson, E De Smet, M Rocchi, A De Paepe, Sven Påhlman & F Speleman, 2006, In: Genes, Chromosomes and Cancer. 45, 2, p. 107-117

    Research output: Contribution to journalArticle

  77. 2005
  78. Fusion of the EWSR1 and ATF1 genes without expression of the MITF-M transcript in angiomatoid fibrous histiocytoma

    Karolin Hansén Hallor, Fredrik Mertens, Yuesheng Jin, Jeanne M Meis-Kindblom, Lars-Gunnar Kindblom, Mikael Behrendtz, Anders Kalén, Nils Mandahl & Ioannis Panagopoulos, 2005 Sep, In: Genes, Chromosomes and Cancer. 44, 1, p. 97-102 6 p.

    Research output: Contribution to journalArticle

  79. Clear cell hidradenoma of the skin - a third tumor type with a t(11;19)-associated TORC1-MAML2 gene fusion

    A Behboudi, M Winnes, Ludmila Gorunova, J J van den Oord, Fredrik Mertens, F Enlund & G Stenman, 2005, In: Genes, Chromosomes and Cancer. 43, 2, p. 202-205

    Research output: Contribution to journalArticle

  80. Formation of der(19)t(1;19)(q23;p13) in acute lymphoblastic leukemia.

    Kajsa Paulsson, Andrea Biloglav, Thoas Fioretos, Felix Mitelman & Bertil Johansson, 2005, In: Genes, Chromosomes and Cancer. 42, 2, p. 144-148

    Research output: Contribution to journalArticle

  81. Intratumor versus intertumor heterogeneity in gene expression profiles of soft-tissue sarcomas.

    Princy Francis, Josefin Fernebro, Patrik Edén, Anna Laurell, Anders Rydholm, Henryk Domanski, Thomas Breslin, Cecilia Hegardt, Åke Borg & Mef Nilbert, 2005, In: Genes, Chromosomes and Cancer. 43, 3, p. 302-308

    Research output: Contribution to journalArticle

  82. 2004
  83. A model for karyotypic evolution in testicular germ cell tumors.

    Attila Frigyesi, David Gisselsson Nord, Gunnar B Hansen, Maria Soller, Felix Mitelman & Mattias Höglund, 2004, In: Genes, Chromosomes and Cancer. 40, 3, p. 172-178

    Research output: Contribution to journalArticle

  84. Identification of cytogenetic subgroups and karyotypic pathways of clonal evolution in follicular lymphomas.

    Mattias Höglund, Laurie Sehn, Joseph M Connors, Randy D Gascoyne, Reiner Siebert, Torbjörn Säll, Felix Mitelman & Douglas E Horsman, 2004, In: Genes, Chromosomes and Cancer. 39, 3, p. 195-204

    Research output: Contribution to journalArticle

  85. MDS/AML-associated cytogenetic abnormalities in multiple myeloma and monoclonal gammopathy of undetermined significance: Evidence for frequent de novo occurrence and multipotent stem cell involvement of del(20q).

    Therese Nilsson, Lars Nilsson, Stig Lenhoff, Lars Rylander, Ingbritt Åstrand-Grundström, Bodil Strömbeck, Mattias Höglund, Ingemar Turesson, Jan Westin, Felix Mitelman, Sten Eirik W Jacobsen & Bertil Johansson, 2004, In: Genes, Chromosomes and Cancer. 41, 3, p. 223-231

    Research output: Contribution to journalArticle

  86. MLL/GRAF fusion in an infant acute monocytic leukemia (AML M5b) with a cytogenetically cryptic ins(5;11)(q31;q23q23).

    Ioannis Panagopoulos, Ashly Kitagawa, Margareth Isaksson, Helena Mörse, Felix Mitelman & Bertil Johansson, 2004, In: Genes, Chromosomes and Cancer. 41, 4, p. 400-404

    Research output: Contribution to journalArticle

  87. Structural integrity and expression of the L3MBTL gene in normal and malignant hematopoietic cells

    D MacGrogan, N Kalakonda, S Alvarez, JM Scandura, P Boccuni, Bertil Johansson & SD Nimer, 2004, In: Genes, Chromosomes and Cancer. 41, 3, p. 203-213

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  88. The chimeric FUS/CREB3l2 gene is specific for low-grade fibromyxoid sarcoma.

    Ioannis Panagopoulos, Clelia Tiziana Storlazzi, Christopher D M Fletcher, Jonathan A Fletcher, Antonio Nascimento, Henryk A Domanski, Johan Wejde, Otte Brosjö, Anders Rydholm, Margareth Isaksson, Nils Mandahl & Fredrik Mertens, 2004, In: Genes, Chromosomes and Cancer. 40, 3, p. 218-228

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